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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Carbamic acid, [(1S)-1-(2R)-oxiranyl-2-phenylethyl]-, 1,1-dimethylethylester

O=C(OC(C)(C)C)N[C@H]([C@H]1OC1)Cc1ccccc1 Request for Quotation
Chemical Name: Carbamic acid, [(1S)-1-(2R)-oxiranyl-2-phenylethyl]-, 1,1-dimethylethylester
CAS Number: 98760-08-8
Product Number: AG0032C9(AGN-PC-0W8LAN)
Synonyms:
MDL No: MFCD00671705
Molecular Formula: C15H21NO3
Molecular Weight: 263.3321

Identification/Properties

Properties
MP:
50-52°C
BP:
398.8°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
263.337g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
6
Exact Mass:
263.152g/mol
Monoisotopic Mass:
263.152g/mol
Topological Polar Surface Area:
50.9A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
305
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (2R,3S)-3-(Tert-Butoxycarbonyl)Amino-1,2-Epoxy-4-Phenylbutane, commonly referred to as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure combining an amino group, an epoxy moiety, and a phenyl group offers a wide range of applications in organic chemistry.In chemical synthesis, (2R,3S)-3-(Tert-Butoxycarbonyl)Amino-1,2-Epoxy-4-Phenylbutane is commonly used as a chiral intermediate for the preparation of complex molecules. This compound serves as a key starting material for the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals due to its ability to introduce chirality and functionality into target molecules.Furthermore, the epoxy group in (2R,3S)-3-(Tert-Butoxycarbonyl)Amino-1,2-Epoxy-4-Phenylbutane offers a reactive site for selective ring-opening reactions, enabling the formation of diverse chemical bonds with high regio- and stereo-selectivity. By strategically incorporating this compound into synthetic routes, chemists can access structurally complex and biologically active compounds efficiently.Overall, (2R,3S)-3-(Tert-Butoxycarbonyl)Amino-1,2-Epoxy-4-Phenylbutane is a valuable tool in chemical synthesis for its ability to introduce chirality, functional groups, and structural diversity into organic molecules, making it a cornerstone in the construction of complex chemical entities.